BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 17942074)

  • 1. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation.
    Ji Y; Jia X; Zhang Q; Yao YG
    Biochem Biophys Res Commun; 2007 Dec; 364(2):238-42. PubMed ID: 17942074
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
    Qu J; Zhou X; Zhang J; Zhao F; Sun YH; Tong Y; Wei QP; Cai W; Yang L; West CE; Guan MX
    Ophthalmology; 2009 Mar; 116(3):558-564.e3. PubMed ID: 19167085
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
    Khan NA; Govindaraj P; Soumittra N; Sharma S; Srilekha S; Ambika S; Vanniarajan A; Meena AK; Uppin MS; Sundaram C; Bindu PS; Gayathri N; Taly AB; Thangaraj K
    Invest Ophthalmol Vis Sci; 2017 Aug; 58(10):3923-3930. PubMed ID: 28768321
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The analysis of mitochondrial DNA haplogroups and variants for Leber's hereditary optic neuropathy in Chinese families carrying the m.14484T >C mutation].
    Meng X; Zhu J; Gao M; Zhang S; Zhao F; Zhang J; Liu X; Wei Q; Tong Y; Zhang M; Qu J; Guan M
    Yi Chuan; 2014 Apr; 36(4):336-45. PubMed ID: 24846978
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
    Tharaphan P; Chuenkongkaew WL; Luangtrakool K; Sanpachudayan T; Suktitipat B; Suphavilai R; Srisawat C; Sura T; Lertrit P
    J Neuroophthalmol; 2006 Dec; 26(4):264-7. PubMed ID: 17204919
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A.
    Wang HW; Jia X; Ji Y; Kong QP; Zhang Q; Yao YG; Zhang YP
    Mutat Res; 2008 Aug; 643(1-2):48-53. PubMed ID: 18619472
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.
    Yu D; Jia X; Zhang AM; Li S; Zou Y; Zhang Q; Yao YG
    PLoS One; 2010 Oct; 5(10):e13426. PubMed ID: 20976138
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
    Zhou X; Zhang H; Zhao F; Ji Y; Tong Y; Zhang J; Zhang Y; Yang L; Qian Y; Lu F; Qu J; Guan MX
    Mol Genet Metab; 2010 Aug; 100(4):379-84. PubMed ID: 20627642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.
    Qu J; Wang Y; Tong Y; Zhou X; Zhao F; Yang L; Zhang S; Zhang J; West CE; Guan MX
    Invest Ophthalmol Vis Sci; 2010 Oct; 51(10):4906-12. PubMed ID: 20435583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.
    Qu J; Zhou X; Zhao F; Liu X; Zhang M; Sun YH; Liang M; Yuan M; Liu Q; Tong Y; Wei QP; Yang L; Guan MX
    Biochim Biophys Acta; 2010 Mar; 1800(3):305-12. PubMed ID: 19733221
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.
    Qian Y; Zhou X; Hu Y; Tong Y; Li R; Lu F; Yang H; Mo JQ; Qu J; Guan MX
    Biochem Biophys Res Commun; 2005 Jul; 332(2):614-21. PubMed ID: 15896721
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation.
    Qu J; Li R; Tong Y; Hu Y; Zhou X; Qian Y; Lu F; Guan MX
    Biochem Biophys Res Commun; 2005 Mar; 328(4):1139-45. PubMed ID: 15707996
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.
    Tong Y; Sun YH; Zhou X; Zhao F; Mao Y; Wei QP; Yang L; Qu J; Guan MX
    Mol Genet Metab; 2010 Apr; 99(4):417-24. PubMed ID: 20053576
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.
    Kaewsutthi S; Phasukkijwatana N; Joyjinda Y; Chuenkongkaew W; Kunhapan B; Tun AW; Suktitipat B; Lertrit P
    Invest Ophthalmol Vis Sci; 2011 Jul; 52(7):4742-8. PubMed ID: 21398275
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.
    Zhang M; Zhou X; Li C; Zhao F; Zhang J; Yuan M; Sun YH; Wang J; Tong Y; Liang M; Yang L; Cai W; Wang L; Qu J; Guan MX
    Mol Genet Metab; 2010; 101(2-3):192-9. PubMed ID: 20728388
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
    Ji Y; Zhang AM; Jia X; Zhang YP; Xiao X; Li S; Guo X; Bandelt HJ; Zhang Q; Yao YG
    Am J Hum Genet; 2008 Dec; 83(6):760-8. PubMed ID: 19026397
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
    Sudoyo H; Suryadi H; Lertrit P; Pramoonjago P; Lyrawati D; Marzuki S
    J Hum Genet; 2002; 47(11):594-604. PubMed ID: 12436196
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].
    Zhou HH; Dai XN; Lin B; Mi H; Liu XL; Zhao FX; Zhang JJ; Zhou XT; Sun YH; Wei QP; Qu J; Guan MX
    Yi Chuan; 2012 Aug; 34(8):1031-42. PubMed ID: 22917908
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients.
    Zhang AM; Jia X; Bi R; Salas A; Li S; Xiao X; Wang P; Guo X; Kong QP; Zhang Q; Yao YG
    PLoS One; 2011; 6(11):e27750. PubMed ID: 22110754
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.
    Qiao C; Wei T; Hu B; Peng C; Qiu X; Wei L; Yan M
    Mol Med Rep; 2015 Aug; 12(2):3067-72. PubMed ID: 25936877
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.